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912279-37-9

2-(N-phenyl-aminooxy)-hex-5-en-3-ol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 912279-37-9 Structure

  • Basic information

    1. Product Name: 2-(N-phenyl-aminooxy)-hex-5-en-3-ol
    2. Synonyms: 2-(N-phenyl-aminooxy)-hex-5-en-3-ol
    3. CAS NO:912279-37-9
    4. Molecular Formula:
    5. Molecular Weight: 207.272
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 912279-37-9.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 2-(N-phenyl-aminooxy)-hex-5-en-3-ol(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-(N-phenyl-aminooxy)-hex-5-en-3-ol(912279-37-9)
    11. EPA Substance Registry System: 2-(N-phenyl-aminooxy)-hex-5-en-3-ol(912279-37-9)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 912279-37-9(Hazardous Substances Data)

912279-37-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 912279-37-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,2,2,7 and 9 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 912279-37:
(8*9)+(7*1)+(6*2)+(5*2)+(4*7)+(3*9)+(2*3)+(1*7)=169
169 % 10 = 9
So 912279-37-9 is a valid CAS Registry Number.

912279-37-9Downstream Products

912279-37-9Relevant articles and documents

Efficient total synthesis of (+)-exo-, (-)-endo-brevicomin and their derivatives via asymmetric organocatalysis and olefin cross-metathesis

Kim, Sung-Gon,Park, Tae-Ho,Kim, Bong Jin

, p. 6369 - 6372 (2006)

The catalytic enantioselective synthesis of (+)-exo-, (-)-endo-brevicomin and their derivatives is described herein. This approach involves the use of the organocatalyzed asymmetric α-aminoxylation of aldehyde, in situ indium mediate allyation and olefin

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